Dynamics of the Skeletal Muscle Secretome during Myoblast Differentiation

被引:237
作者
Henningsen, Jeanette [1 ,2 ,3 ]
Rigbolt, Kristoffer T. G. [1 ]
Blagoev, Blagoy [1 ]
Pedersen, Bente Klarlund [2 ,3 ]
Kratchmarova, Irina [1 ]
机构
[1] Univ So Denmark, Ctr Expt BioInformat, Dept Biochem & Mol Biol, DK-5230 Odense M, Denmark
[2] Univ Copenhagen, Ctr Inflammat & Metab, Dept Infect Dis, Rigshosp,Fac Hlth Sci, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen, Copenhagen Muscle Res Ctr, Rigshosp, Fac Hlth Sci, DK-2100 Copenhagen, Denmark
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
GROWTH-FACTOR-BETA; NEURAL CHEMOREPELLENT SEMA3A; IGF-BINDING-PROTEINS; TGF-BETA; SATELLITE-CELLS; QUANTITATIVE PROTEOMICS; ENDOCRINE ORGAN; AMINO-ACIDS; IN-VITRO; EXPRESSION;
D O I
10.1074/mcp.M110.002113
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During recent years, increased efforts have focused on elucidating the secretory function of skeletal muscle. Through secreted molecules, skeletal muscle affects local muscle biology in an auto/paracrine manner as well as having systemic effects on other tissues. Here we used a quantitative proteomics platform to investigate the factors secreted during the differentiation of murine C2C12 skeletal muscle cells. Using triple encoding stable isotope labeling by amino acids in cell culture, we compared the secretomes at three different time points of muscle differentiation and followed the dynamics of protein secretion. We identified and quantitatively analyzed 635 secreted proteins, including 35 growth factors, 40 cytokines, and 36 metallopeptidases. The extensive presence of these proteins that can act as potent signaling mediators to other cells and tissues strongly highlights the important role of the skeletal muscle as a prominent secretory organ. In addition to previously reported molecules, we identified many secreted proteins that have not previously been shown to be released from skeletal muscle cells nor shown to be differentially released during the process of myogenesis. We found 188 of these secreted proteins to be significantly regulated during the process of myogenesis. Comparative analyses of selected secreted proteins revealed little correlation between their mRNA and protein levels, indicating pronounced regulation by posttranscriptional mechanisms. Furthermore, analyses of the intracellular levels of members of the semaphorin family and their corresponding secretion dynamics demonstrated that the release of secreted proteins is tightly regulated by the secretory pathway, the stability of the protein, and/or the processing of secreted proteins. Finally, we provide 299 unique hydroxyproline sites mapping to 48 distinct secreted proteins and have discovered a novel hydroxyproline motif. Molecular & Cellular Proteomics 9:2482-2496, 2010.
引用
收藏
页码:2482 / 2496
页数:15
相关论文
共 79 条
[1]   The chemorepulsive activity of secreted semaphorins is regulated by furin-dependent proteolytic processing [J].
Adams, RH ;
Lohrum, M ;
Klostermann, A ;
Betz, H ;
Puschel, AW .
EMBO JOURNAL, 1997, 16 (20) :6077-6086
[2]  
[Anonymous], 2007, R LANG ENV STAT COMP
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]   IGF-binding proteins - the pieces are failing into place [J].
Bach, LA ;
Headey, SJ ;
Norton, RS .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2005, 16 (05) :228-234
[5]   Pattern of metalloprotease activity and myofiber regeneration in skeletal muscles of mdx mice [J].
Bani, Cristiane ;
Lagrota-Candido, Jussara ;
Pinheiro, Douglas Florindo ;
Correa Leite, Paulo Emllio ;
Salimena, Maria Cristina ;
Henriques-Pons, Andrea ;
Quirico-Santos, Thereza .
MUSCLE & NERVE, 2008, 37 (05) :583-592
[6]   MT1-MMP controls tumor-induced angiogenesis through the release of semaphorin 4D [J].
Basile, John R. ;
Holmbeck, Kenn ;
Bugge, Thomas H. ;
Gutkind, J. Silvio .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (09) :6899-6905
[7]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[8]   MyoD and the transcriptional control of myogenesis [J].
Berkes, CA ;
Tapscott, SJ .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (4-5) :585-595
[9]   Quantitative proteomics to study mitogen-activated protein kinases [J].
Blagoev, Blagoy ;
Mann, Matthias .
METHODS, 2006, 40 (03) :243-250
[10]   Combined use of RNAi and quantitative proteomics to study gene function in Drosophila [J].
Bonaldi, Tiziana ;
Straub, Tobias ;
Cox, Juergen ;
Kumar, Chanchal ;
Becker, Peter B. ;
Mann, Matthias .
MOLECULAR CELL, 2008, 31 (05) :762-772